Overview
Nicola Brunetti-Pierri is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Brunetti-Pierri and is rated as an Experienced provider by MediFind in the treatment of Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A). His top areas of expertise are Pyruvate Decarboxylase Deficiency, Crigler-Najjar Syndrome, Rotor Syndrome, and Argininosuccinic Aciduria.
His clinical research consists of co-authoring 209 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A).
Insurance
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Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Elite
- Argininosuccinic Aciduria
- Crigler-Najjar Syndrome
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Myhre Syndrome
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- Distinguished
- Achalasia Microcephaly Syndrome
- Atresia of Small Intestine
- Cortical Dysplasia
- Hypotonia
- Microcephaly
- Multiple Sulfatase Deficiency
- Advanced
- Acromicric Dysplasia
- Allan-Herndon-Dudley Syndrome
- Alpha-1 Antitrypsin Deficiency (AATD)
- Bardet-Biedl Syndrome
- Bilateral Perisylvian Polymicrogyria
- Blepharophimosis
- Experienced
- Aplasia Cutis Congenita
- Arthrogryposis Multiplex Congenita
- Autism Spectrum Disorder
- Brachydactyly
- Brachydactyly Mononen Type
- C Syndrome